Validation Engineer

We are looking for a detail-oriented Validation Engineer to join our client based in Philadelphia on a 12 months contract. You will be responsible for ensuring that manufacturing processes, equipment, and systems meet the required standards and regulations.

Key Responsibilities:

• Develop and execute validation protocols (IQ, OQ, PQ) for equipment, processes, and systems.
• Conduct risk assessments and develop mitigation strategies.
• Ensure compliance with regulatory requirements (FDA, EMA, etc.).
• Conducting regular inspections, performing calibrations, identifying areas for improvement, and alerting management of potential issues.
• Collaborate with cross-functional teams to support validation activities.
• Maintain accurate and detailed documentation of validation activities.
• Investigate and resolve validation-related issues.
• Participate in continuous improvement initiatives.

Required Qualifications:

• Bachelor’s degree in Engineering, Life Sciences, or a related field.
• Minimum of 5 years of experience in validation within the pharmaceutical industry.
• Strong knowledge of regulatory requirements and guidelines.
• Strong attention to detail and organizational skills.

Contract:

• 40 hours per week
• Start Date: ASAP
• Contract Length: 12 months
• Philadelphia, PA
• W2 only